Methods for detecting and quantifying binding and inhibition of binding of species to nucleic acids

ABSTRACT

The invention features methods for detecting and quantifying the binding or inhibition of binding of species to biopolymers, e.g., nucleic acids. The invention is based on the use of probes that have magnetic relaxation properties that are affected by the presence of paramagnetic metal ions, e.g., Mn 2+ . Any class of biopolymer that binds metal ions at its active site or uses metal ion cofactors can be studied using these methods.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit of priority from U.S. Provisional Application No. 60/332,969, filed Nov. 6, 2001, hereby incorporated by reference.

BACKGROUND OF THE INVENTION

The invention relates to the fields of drug discovery and nuclear magnetic resonance spectroscopy.

Nucleic acids (DNA and RNA) are biopolymers in which each monomer contains a negatively charged phosphate ester group. This large negative charge is balanced by interaction of the nucleic acid with small cationic species, including protonated amines, and monovalent and divalent metal ions. In addition to non-specific electrostatic interactions, structured nucleic acids have specific metal ion binding sites. Examples of specific divalent metal ion binding by RNA molecules can be seen in the group III-V intron of the tetrahymina ribozyme, ribosomal RNA, and RNA aptamers. Such interactions may be mediated by direct coordination of the bases or phosphates to the metal ion, or by hydrogen bonding between water molecules coordinated to the metal ion and the nucleotide bases.

Divalent metal ions can be bound by either specific interactions with discrete metal binding sites or non-specifically via coulombic interaction. For non-specific interactions, binding is described by the polyelectrolyte condensation model. Binding affinities are dependant on the ionic strength of the solution and the nature of the cationic form of the supporting electrolyte. This dependence on the nature and concentration of the supporting electrolyte is to be expected since the divalent ion will have to compete with the electrolyte cation for both specific and non-specific interactions. Non-specific affinities can be represented by interactions of Mg²⁺ with poly-uridine (poly-U). In 10 mM NaCl, 96 μM Mg²⁺, the apparent association constant for poly-U/Mg binding is reported as 1.86×10³ M⁻¹nt⁻¹, where nt is the number of nucleotides in the strand. When other bases are incorporated into the RNA strand, binding of the metal to the bases is possible. Under similar conditions to those of the poly-U study, poly-A has a reported Mg²⁺ binding affinity of 10.7×10³ M⁻¹nt⁻¹, a 5.7 fold increase over poly-U. This difference must be attributed to contributions from base/metal interactions, since the two nucleic acids share the same charge distribution along their backbones. Specific metal binding sites having affinities in the micromolar range have been reported for transfer RNAs and the hammerhead ribozyme. Up to 8 Mn²⁺ ions bind to the Hammerhead ribozyme with K_(D) values ranging from 4 to 500 μM.

Since divalent metal ions are necessary structural elements of some molecules of RNA and since the RNA molecules exchange bound ions with ions free in the bulk solution, sites for binding metal ions are natural candidates for drug targets. Aminoglycoside antibiotics are believed to act by displacing divalent metal ions from specific binding sites on RNA. Aminoglycosides are reported to displace Mg²⁺ from specific sites on a variety of RNA molecules including a model of the ribosomal A, the hammerhead ribozyme, the tetrahymina group I intron, and RNase P.

The magnetic relaxation properties of NMR active nuclei can be very sensitive to paramagnetic metal ions. Thermodynamic and structural aspects of macromolecules that bind metal ions have been studied by exploiting this effect. In the majority of works, the effects of the paramagnetic metal ion on the magnetic resonances of ¹H of the biological molecule have been determined in order to study the geometry of the metal binding site. In addition, there have been a more limited number of studies where the metal binding sites have been examined using external small species such as water or fluoride ion.

Paramagnetic relaxation enhancement of the magnetic resonance of ¹H nuclei of solvent water has been used to study metal binding by a variety of biological macromolecules qualitatively. This approach has been used to characterize the binding of Mn²⁺ to transfer RNA and ribosomal RNA among other molecules. Another approach for paramagnetic relaxation enhancement that has seen limited use is the use of ¹⁹F fluoride as a probe. Relaxation enhancements of this resonance by superoxide dismutases have been reported. Metal ion binding studies where the perturbations observed are of the macromolecular ¹H resonances have also been reported. Molecules studied include ribozymes and smaller RNA fragments. Water ¹H resonances, however are not very sensitive to paramagnetic relaxation, and ¹⁹F measurements require ¹⁹F NMR.

There exists a need for sensitive methods for measuring the binding and inhibition of binding of species to nucleic acids. These methods may find use in the field of drug discovery.

SUMMARY OF THE INVENTION

The invention provides methods for detecting and quantifying the binding or inhibition of binding of species, e.g., candidate therapeutic agents, to biopolymers, e.g., nucleic acids. The invention is based on the use of probes that have magnetic relaxation properties that are affected by the presence of paramagnetic metal ions. Although the following description focuses on nucleic acids, any class of biopolymer that binds metal ions at its active site or uses metal ion cofactors can be studied using these methods.

In one aspect, the invention features a method of detecting the binding of a species to a nucleic acid that includes the steps of measuring a magnetic relaxation property of a probe in a first solution using nuclear magnetic resonance spectroscopy, wherein the first solution includes the nucleic acid, a first concentration of the species, a paramagnetic metal ion, and the probe; measuring the magnetic relaxation property of the probe in a second solution using nuclear magnetic resonance spectroscopy, wherein the second solution includes the nucleic acid, a second concentration of the species, a paramagnetic metal ion, and the probe; and comparing the relaxation properties measured, wherein a difference in the relaxation properties indicates the binding of the species to the nucleic acid. In one embodiment, the magnetic relaxation properties of the probe are correlated with the first and second concentrations of the species, thereby quantifying the binding of the species to the nucleic acid.

The invention further features a method of detecting the binding of a paramagnetic metal ion to a nucleic acid including the steps of measuring a magnetic relaxation property of a probe in a first solution using nuclear magnetic resonance spectroscopy, wherein the first solution includes a first concentration of the paramagnetic metal ion, the nucleic acid, and the probe; measuring the magnetic relaxation property of the probe in a second solution using nuclear magnetic resonance spectroscopy, wherein the second solution includes a second concentration of the paramagnetic metal ion, the nucleic acid, and the probe; and comparing the relaxation properties measured, wherein a difference in the relaxation properties indicates the binding of the paramagnetic metal ion to the nucleic acid. In one embodiment, the magnetic relaxation properties of the probe are correlated with the first and second concentrations of the nucleic acid, thereby quantifying the binding of the paramagnetic metal ion to the nucleic acid.

In another aspect, the invention features a method of determining the effect of a first species on the binding of a second species to a nucleic acid including the steps of measuring a magnetic relaxation property of a probe in a first solution using nuclear magnetic resonance spectroscopy, wherein the first solution includes a first concentration of the first species, the nucleic acid, the second species that binds to the nucleic acid, a paramagnetic metal ion, and a probe; measuring the magnetic relaxation property of the probe in a second solution using nuclear magnetic resonance spectroscopy, wherein the second solution includes a second concentration of the first species, the nucleic acid, the second species, the paramagnetic metal ion, and the probe; and comparing the relaxation properties measured, wherein a difference in the relaxation properties indicates the inhibition of the binding of the second species to the nucleic acid. In one embodiment, the magnetic relaxation properties of the probe are correlated with the first and second concentrations of the first species, thereby quantifying the effect of the first species on the binding of the second species to the nucleic acid.

The invention also features a method of detecting the availability of a paramagnetic metal ion in a solution comprising a nucleic acid including the steps of providing a solution comprising the nucleic acid, a probe, and the paramagnetic metal ion; and measuring a magnetic relaxation property of the probe in the solution using nuclear magnetic resonance spectroscopy, wherein the magnitude of the magnetic property is indicative of the availability of the paramagnetic ion in the solution.

In various embodiments of the above aspects, the first (or second) concentration of a species or ion may be 0.0 μM. In addition, a second concentration may be lower or higher than a first concentration, and a second solution may be formed by the addition or removal of species or ions from the first solution. Exemplary species include metal ions (e.g., Mg²⁺) and candidate therapeutic agents (e.g., proteins, peptides, or fragments thereof). Desirably a candidate therapeutic agent is selected from a molecular library (e.g., a combinatorial library). The nucleic acid may be RNA or DNA and may also be double-stranded or single stranded. Exemplary paramagnetic metal ion include, without limitation, Mn²⁺, Fe²⁺, Fe³⁺, Co²⁺, Ni²⁺, and a lanthanide ion. In other embodiments, the paramagnetic ion is bound to the nucleic acid. Desirably, the probe includes an X—H bond, wherein X is an NMR-active nucleus. In desirable embodiments, X is ³¹P, such as in methylphosphite or ethylphosphite. The probe may also be an alkylphosphonite, e.g., ethylphosphonite.

In addition, the magnetic relaxation properties of X may be indirectly detected using X edited, ¹H detected NMR spectroscopy. In various embodiments, the magnetic relaxation property is the T₂ relaxation of a nucleus of the probe. Desirably, the measuring of said magnetic relaxation properties of X proceeds by the steps of using a pulse sequence to transfer coherent magnetization originating on the ¹H nucleus to the X nucleus by Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) techniques prior to a T₂ delay; providing a T₂ delay; and transferring the remaining coherence back to the ¹H nucleus for detection using a reverse INEPT series of pulses.

In another aspect, the invention features a kit for screening for species that bind to or inhibit binding to nucleic acids including a nucleic acid, a paramagnetic metal ion, and a probe, as described herein. The kit may further include an NMR spectrometer.

By “probe” is meant any molecule or species having at least one NMR active nucleus that undergoes a significant increase in transverse relaxation time (T₂) when in a solution containing a paramagnetic metal ion. Examples of NMR-active nuclei include, but are not limited to, ¹H, ¹³C, ³¹P, ¹⁵N, ¹⁷O, and ¹⁹F (see Yoder, C. H., et al. Introduction to Multinuclear NMR, Cummings:Menlo Park 1987, pp 317-319). Desirable probes include those that contain X—H bonds, where X is a non-hydrogen NMR-active nucleus. More desirably the probes contain P—H bonds. Particularly desirable probes are methylphosphite and ethylphosphonite. Other suitable probes contain only one NMR-active nucleus of an element other than hydrogen, e.g., ¹⁵N or ³¹P.

By “species” is meant a molecule, atom, radical, ion, or metal ion. Desirable species include, but are not limited to, members of molecular libraries, inorganic compounds, synthetic molecules, natural products, antibiotics, drugs, drug candidates, derivatives of natural products, proteins, peptides, fragments of proteins, and Mg²⁺.

By “nucleic acid” is meant substituted or unsubstituted RNA or DNA. Desirable nucleic acids are RNA molecules.

By “NMR-active nucleus” is meant a nucleus having a non-zero net nuclear spin.

By “biopolymer” or “biological polymer” is meant a protein, polypeptide, nucleic acid, or polysaccharide. The biopolymer may include naturally occurring components or synthetically modified components. In desirable embodiments, the biopolymer is a nucleic acid.

By “candidate therapeutic agent” is meant a chemical species that is identified by an assay as potentially having therapeutic efficacy for a specified condition. Exemplary candidate therapeutic agents include, without limitaion, natural and synthetic organic compounds, natural or synthetic inorganic compounds, natural or synthetic peptides or polypeptides, and nucleic acids.

By “bound to the nucleic acid” is meant coordinated to the nucleic acid and not free in solution.

By “availability” of species in solution is meant the ability of a probe to interact with the species to an extent that a magnetic property of the probe is altered. Species free in solution have a greater availability than those coordinated to a nucleic acid.

Other features and advantages of the invention will be apparent from the following description and the claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B are schematic representations of chemical structures of methylphosphite (MeOPH) and ethylphosphonite (EtPH), respectively.

FIG. 2 is a schematic representation of one-dimensional pulse sequences for measuring ³¹P T₂ values using ¹H detection. Broad and narrow bars represent 180- and 90-degree pulses, respectively.

FIG. 3 is a graph showing the intensity (i) of the ¹H signal of ethylphosphite (EtOPH) obtained using the pulse sequence of FIG. 2 as a function of the length of the CPMG pulse train.

FIG. 4 is a graph showing the inverse of the T₂ relaxation time (1/T₂) of EtOPH ³¹P with and without RNA present as a function of the concentration of Mn²⁺.

FIG. 5 is a graph showing the inverse of the T₂ relaxation time (1/T₂) of EtOPH ³¹P in the presence of 5.3 μM Mn²⁺ as a function of RNA concentration.

FIG. 6 is a graph showing the concentration of free Mn²⁺ in the presence of 3.6 μM of RNA as a function of the concentration of the nucleic acid binding compound MES 10094.

FIG. 7 is a graph showing the effect of RNA concentration on paramagnetic T₂ relaxation enhancement by Mn²⁺.

FIG. 8 is a graph showing the effect of a 27-nt A-site RNA construct on probe ion relaxation enhancement by Mn²⁺.

FIG. 9 is a graph showing the displacement of bound Mn²⁺ from a 27-nt A-site RNA construct by neomycin.

FIG. 10 is a graph showing the effect of electrolyte concentration on relaxation enhancement, expressed as a fraction of enhancement expected in the absence of RNA, in solutions of a 27-nt A-site RNA construct and Mn²⁺.

FIG. 11 is a graph showing Mn²⁺ binding by a 27-nt A-site RNA construct under different salt concentrations.

FIG. 12 is a schematic description of a one dimensional pulse sequence for measuring phosphite ³¹P T₂ values. Coherence originating on the phosphorus bound proton (¹H—P) nucleus is transferred to the ³¹P nucleus using a series of inept pulses. After a series of CPMG 180 degree refocusing pulses (³¹P frequency), the remaining signal is returned to the ¹H—P nucleus for detection using a second series of inept pulses. The transverse relaxation times (T₂) were determined from the slopes of the linear plots of log(i) versus t where i is the maximum intensity of the resonance, and t is the time between the two inept series of pulses (t=4nδ). Narrow and broad lines represent 90 and 180 degree pulses on the indicated channel. A 90 degree ³¹P pulse and two homospoil pulses are inserted into delay 1 to remove artifacts arising from residual magnetization remaining between transients. All pulse phases are zero unless noted otherwise. Delays in the inept 1 and inept 2 portion of the sequence (A) are equal to 1/4 J. The delay between CPMG pulses (δ) was 4 ms. The T₂ delay was varied by changing the number of times through the CPMG cycle (n). Phase cycles were as follows: a=(1,1,1,1,3,3,3,3), b=(2), c=(3,3,3,3,3,3,3,3,1,1,1,1,1,1,1,1), d=(0,2), e=(0,0,2,2), and obs=(2,0,0,2,0,2,2,0).

FIG. 13A is a schematic depiction of RRE1, RRE2, and A-site hairpin structures.

FIG. 13B is a schematic depiction of neomycin b.

FIG. 13C is a schematic depiction of RSG1.2.

FIG. 14 is a semi-log plot showing the effects of [Mn²⁺] on ³¹P transverse relaxation rates (R_(2,obs)) of phosphite dianion (HPO₃ ²⁻, represented by the X within the error bars) and methyl phosphite anion (CH₃OP(H)O₂ ⁻, represented by a +), corrected for diamagnetic relaxation rate (R_(2,dia)). R₂ of HPO₃ ²⁻ is a factor of ten more sensitive to [Mn²⁺] than the R₂ of MeOPH. Lines show behavior predicted for relaxation enhancement proportional to [Mn²⁺].

FIG. 15 is a graph of the effect of A-site RNA on free Mn²⁺ (5 mM PIPES, pH 7.2, 5 mM MeOPH, K⁺ salts). The line represents behavior predicted for 7 independent binding sites having K_(d,Mn)=25 μM.

FIG. 16 is a graph of the effect of [K⁺] on free Mn²⁺ in solutions of A-site (27 μM) and Mn²⁺ (16 μM), as determined from R₂ data (FIG. 14).

FIG. 17 is a graph of the effect of [Mg²⁺] on MeOPH relaxation in solutions of RRE1 (20 μM) in 25 mM K⁺ (filled triangles) or 100 mM K⁺ (open diamonds) and Mn²⁺ (3 μM). Solid lines show behavior predicted by the K_(d) and n values in Table 1.

FIG. 18 is a graph of the effect of neomycin b on the relaxation rate (R₂) of the HPO₃ ²⁻ ³¹P signal in solutions of A-site RNA (2.7 uM), Mn²⁺ (0.11 uM), and 100 mM K⁺.

FIG. 19 is a graph of the effect of RSG1.2 on Mn²⁺ binding by either 2.7 μM RRE1 (filled triangles) or 3.0 μM RRE2 (open diamonds) in 100 mM K⁺. Values were normalized to the R₂ value, obtained upon addition of 2 mM Mg²⁺

FIG. 20 is a graph of the effect of [RRE1] (filled triangles) and [RRE2] (open diamonds) on fluorescence polarization of TAMRA labeled RSG1.2.

DETAILED DESCRIPTION OF THE INVENTION

The invention features methods for detecting binding or inhibition of binding of a species to a biopolymer, e.g., a nucleic acid. Certain chemical species can be used as probes for studying metal coordination by such a biopolymer. The presence of paramagnetic metal ions affects the magnetic relaxation properties of nuclei in these probes as measured, for example, by NMR. The accessibility of paramagnetic metal ions to the probe in solution correlates with the magnitude of these effects on magnetic relaxation.

Certain biopolymers bind metal ions in solution. The addition or removal of species that affect the quantity of metal ions bound to a biopolymer, e.g., a nucleic acid, can be studied using a suitable probe. Methods based on this phenomenon can be used to study, for example, binding of metal ions directly to nucleic acids, species that bind to nucleic acids and displace metal ions, and species that inhibit the binding of other species to nucleic acids. The methods may also be used to study species that expose or conceal metal ions bound to biopolymers to allow or prevent interaction with a probe species, respectively.

Paramagnetic Metal Ions

Metal ions bound in vivo to biopolymers can usually be replaced with paramagnetic metal ions. For example, magnesium ions (Mg²⁺) are normally found in vivo in nucleic acid complexes and can usually be replaced with, for example, manganous ion (Mn²⁺). Ions such as Mn²⁺ often support the structural and reactivity requirements of nucleic acids and their complexes for processing and binding proteins. The chemistry of Mn²⁺ also closely approximates that of Mg²⁺. These two cations show similar preferences for six coordination sites and have similar bond energies and Lewis acidities. While the chemistry of Mn²⁺ and Mg²⁺ are similar, their magnetic properties are very different. Mg²⁺ is diamagnetic (having no unpaired electrons), and Mn²⁺ is paramagnetic (containing five unpaired electrons). Additional exemplary paramagnetic ions that are useful in the methods described herein include, without limitation, Fe²⁺, Fe³⁺, Co²⁺, Ni²⁺, or a lanthanide ion.

Probes

Magnetic resonances of certain nuclei can be highly sensitive to paramagnetic ions, and compounds containing these NMR-active nuclei can be used as probes for the presence of paramagnetic metal ions. For example, the ³¹P nuclei of certain anionic materials including methylphosphite are remarkably sensitive to magnetic T₂ relaxation by Mn(H₂O)₆ ²⁺ (or free Mn²⁺). Changes in the ³¹P NMR transverse relaxation rates of MeOPH can be used, for example, to detect and quantify the concentration of Mn²⁺ in aqueous solutions at concentrations below 1μM.

Previous work has measured magnetic relaxation of molecules in close proximity to paramagnetic metal ions, but significant differences exist between the methods of this invention and those of the prior art. In previous approaches, it is the magnetic resonances of the biopolymers, e.g., nucleic acids, themselves that are observed. Methods that center on measuring the effect of metal ions have on the resonances of the biopolymers are unlikely to develop into reasonable screens for drug activity. Such a method would require that the biopolymers be present in the solutions at concentrations of hundreds of ELM or above. Since the analyte must also be present at this concentration, the effects of weak interactions (K_(d)˜100 μM) cannot be distinguished from those of stronger interactions. Since compounds that only weakly interact are unlikely to make good drug candidates, and weak binders cannot be differentiated from stronger binders, these methods are of limited use. The concentration limitations also mean that drugs with lower solubilities cannot be studied by these methods. Since the methods of the present invention observe the resonances of a probe, they are not limited to working with high concentrations of biological species and can be used to screen for drug hits at more physiological conditions.

Another limitation on methods where macromolecular resonances are observed arises from the spectral overlap of these resonances: resolution and assignment of these resonances would require multi-dimensional spectroscopy of isotopically labeled samples. An additional benefit arises for the methods described herein since they do not require the assignment of the macromolecular resonance chemical shifts. Macromolecules have many nuclei of a given element, e.g., H, C, N, or P, that may be present in chemical environments that only slightly differ. Since small differences in chemical environment give rise to small differences in chemical shift, the precise assignment of one nucleus out of the many similar nuclei is difficult.

The probes described herein form a complex with the paramagnetic metal ions. This complex is weakly bound relative to complexes of the metal ions and nucleic acids. Complexation of the probe to the metal ion affects the magnetic relaxation properties of the probe. To achieve the maximum sensitivity in methods that measure metal ion availability in solution, interactions between the probe are paramagnetic metal ion are desirable minimized when the ion is bound to a biopolymer. For example, one method to minimize the interaction of the probe with metal ions bound to nucleic acids is to make the probe anionic. Since the metal ion is sequestered by a poly-anionic nucleic acid, the overall charge will be highly negative and repel the anionic probe ion. Thus, changes in the magnetic relaxation properties by the sequestered metal ion are not observed. If association with monovalent cations neutralizes the anionic charge of the nucleic acid, then relaxation enhancement by the nucleic acid/Mn²⁺ complex is possible. In methods that measure the accessibility of a metal ion bound to a biopolymer, however, the probe desirably interacts with the bound metal. For example, the probe may be of the opposite charge to the biopolymer, or it may be neutral.

Exemplary probes are shown in FIG. 1. These probes have at least one P—H moiety and at least one terminal P—O moiety, examples include alkyl phosphite anions (e.g., methylphosphite, MeOPH, and ethylphosphite, EtOPH) and phosphonite anions (e.g., ethylphosphonite, EtPH). These probe ions are far more sensitive to metal ions than the water ¹H resonance and have the advantage over fluoride of allowing ¹H detection with isotope editing (Dwek, R. A. Nuclear Magnetic Resonance in Biochemistry Clarendon:Oxford 1973).

NMR

Nuclear magnetic resonance (NMR) spectroscopy is a widely used technique to study chemical and structural properties of species. The ability to detect magnetic relaxation rates, e.g., from T₁ and T₂ relaxations, provides a route to probe the environment of a particular nucleus.

For probes containing X—H bonds, the T₂ relaxation of the X nucleus can be monitored using ¹H detection and isotope editing. For example, a pulse sequence for a one-dimensional NMR experiment used to determine changes in ³¹P T₂ of phosphites or phosphonites with indirect detection is shown in FIG. 2. In this example, coherent magnetization originating on the ¹H is transferred to the ³¹P via inept sequence (a). The sample is pulsed with a series of 180-degree phosphorus re-focusing pulses (during the CPMG train), and magnetization is transferred back to the ¹H nucleus for detection (inept sequence (b)). Delays between pulses in the two inept sequences are set to 1/4 J. Pulse phases are those described by Farrow et al., for a ¹⁵N T₂ correlation experiment (Farrow, N. A. et al. Biochemistry, 1994, 33:5984-6003). The number of 180-degree phosphorus refocusing pulses during the CPMG portion of the sequence and the delay between these pulses can be adjusted to alter the total time in the CPMG train. During this time (which is called the T₂ time) transverse relaxation of the ³¹P nucleus occurs, leading to a diminution of the intensity (i) of the observed signal. For example, the effect of variations in T₂ time on the intensity of the phosphite ¹H signal of EtOPH in a solution containing 5 μM Mn²⁺ is presented in FIG. 3. In this example, the delay between ³¹P 180-degree pulses was held fixed at 200 μs, and the number of pulses increased as the length of the CPMG pulse train increased. For example, the shortest time corresponds to 8 CPMG pulses, and the longest time corresponds to 160 pulses. The transverse relaxation time of the ³¹P nucleus of the probe under these conditions is equal to the magnitude of the slope of the plot. While this particular example is for ³¹P nuclei, the technique is generally applicable to other NMR-active nuclei X that form strong X—H bonds.

The sensitivity of the technique depends, e.g., on the reproducibility of the instrumentation, sample variability, and any paramagnetic impurities or dissolved oxygen present in the sample. The sensitivity also depends strongly on the charge of the biopolymer. For example for RNA in low salt solutions, changes in Mn²⁺ concentration of ˜300 nM are detected with suitable reproducibility.

Applications

The methods of the present invention can be used to study the relative or absolute increase or decrease in the accessibility of metal ions in solution.

The ability to detect and quantify the concentration of free paramagnetic metal ions in solution provides methods, for example, to screen a series of drug candidates for species that bind to biopolymers, e.g., a nucleic acid, or inhibit the binding of other species to biopolymers, to determine the stoichiometry of metal ions binding to biopolymers, or to determine relative or absolute affinities of species binding to biopolymers. The ability to detect and quantify the accessibility of a metal ion bound to a biopolymer provides methods, for example, to screen for ligands that bind or inhibit the binding of species to the metal or biopolymer.

In one embodiment, species that bind to nucleic acids displace bound paramagnetic metal ions and cause an increase in the concentration of paramagnetic metal ions free in solution. This increase in concentration is measured, for example, by NMR as an increase in the T₂ relaxation rate of nuclei in a probe. The T₂ relaxation rates are then correlated with the concentration of species that binds to nucleic acid to detect or quantify the amount of paramagnetic metal ions freed upon binding of the species to nucleic acid. The species that binds the nucleic acid may be, e.g., a synthetic organic molecule, a peptide, or a protein.

In another embodiment, nucleic acid is added to a solution of free paramagnetic metal ions. The ions then bind to the nucleic acid. This binding is measured, for example, by NMR as a decrease in the T₂ relaxation rate of nuclei in a probe. The change in the rate of relaxation of nuclei in the probe is then correlated with the concentration of nucleic acid to detect or quantify the binding of paramagnetic metal ions to the nucleic acid.

In still another embodiment, a species that potentially inhibits the binding of other species, e.g., a protein, to nucleic acids is added to a solution containing a species bound to a nucleic acid and paramagnetic metal ions. Desirable proteins for binding inhibition include, without limitation, the Hu antigens and AUF1 (Wilson, G. M. et al. J. Biol. Chem. 2001, 276:8695-8704). The inhibiting species reduces the concentration of the other species bound to the nucleic acid, which allows paramagnetic metal ions to bind to the nucleic acid. The binding of paramagnetic metal ions to the nucleic acid reduces the concentration free in solution. The inhibition of binding of the species to the nucleic acid is measured, for example, by NMR as a decrease in the T₂ relaxation rate of nuclei in a probe caused by the reduced concentration of metal ions in solution. The change in the rate of relaxation of the nuclei in the probe is then correlated with the concentration of the inhibiting species to detect or quantify the inhibition of species binding to nucleic acid.

EXAMPLES

The following examples are provided merely to illustrate various features and other details of the invention and should not be construed as limiting.

In Examples 1-15, the effects of RNA on equilibrium concentrations of Mn²⁺ are determined using a phosphite probe ion (either Methyl phosphite, MeOPH, or Ethyl phosphite, EtOPH). Typically, samples of MeOPH were prepared at (5-10 mM) in PIPES buffer (5-10 mM), which is known not to interfere with metal ion availability (Kandegedara A. et al. Anal. Chem. 1999, 71:3140:3144). Aliquots of stock solutions were evaporated in vacuo and reconstituted in D₂O (all experiments used D₂O as solvent). Samples were treated with aliquots of Mn²⁺ in the presence and in the absence of the RNA of interest.

Example 1 Synthesis of MeOPH and EtOPH

MeOPH was prepared by partial hydrolysis of dimethyl phosphite in aqueous base. Dimethyl phosphite (for MeOPH) or diethyl phosphite (for EtOPH) (Aldrich) was dissolved in deionized water, and the resulting solution was neutralized by addition of an equivalent of either sodium hydroxide (to prepare the sodium salt) or potassium hydroxide (to prepare the potassium salt). The progress of the reaction was monitored using a pH meter. The rate of addition was such that the temperature of the solution was not allowed to exceed ˜60° C. On a gram scale (˜2 M concentration), the process is complete in ˜5 minutes. Aliquots of the sample were then evaporated in vacuo to give a colorless powder that could be dissolved into D₂O for spectroscopic studies. The phosphorus bound proton did not exchange readily with those of the solvent.

Example 2 Synthesis of EtPH

EtPH was prepared by hydrolysis of ethyl-dichloro-phosphine. To a beaker of deionized water in an ice bath was added the contents of a one-gram ampoule of ethyl-dichloro-phosphine with stirring. A vigorous exothermic reaction ensued. The sample was neutralized with aqueous base, and aliquots were evaporated in vacuo.

Example 3 Measurement of T₂ Relaxation Rates with NMR Spectroscopy

The ³¹P T₂ was measured for each sample by varying the length (number of pulses) of the CPMG portion of the pulse sequence in FIG. 2 and determining the effect of this change on the intensity (i) of the signals. Plots of ln(i) versus time (as seen in FIG. 3) were linear with a slope equal to the negative of the ³¹P T₂. The d1 delay was typically 5 to 20 seconds, and delays in the inept and reverse inept parts of the sequence were set to a value equal to 1/4 J, where J is the ¹H—³¹P coupling constant. Delays between pulses in the CPMG train varied from 50 to 500 microseconds.

Example 4 Mn²⁺ Binding Properties of a 38 Nucleotide RNA

A TNF-α mRNA construct binds divalent metal ions in a way that poly-U does not (Wilson, G. M. et al. J. Biol. Chem. 2001, 276:8695-8704). Complex formation between the RNA binding protein AUF1 and its target RNA is inhibited by Mg²⁺, and RNA binds Ca²⁺ and Mn²⁺ as well as Mg²⁺. These results indicate that metal ions are released from specific sites on RNA when bound to AUF1.

A solution of EtOPH (5 mM) in D₂O was prepared and aliquots were treated with aliquots of Mn²⁺. Similar samples were prepared but with a 38 nt ARE RNA construct at a concentration of 200 μM. The sequence of this RNA was identical to that reported (Wilson, G. M. et al. J Biol. Chem. 2001, 276:8695-8704) to bind divalent metal ions. In the absence of the RNA, the measured value of the ³¹P T₂, obtained as described in Example 3, decreased with the addition of metal ion. When the reciprocal of T₂ of the ³¹P nucleus was plotted versus Mn²⁺ concentration, a linear correlation was obtained (open diamonds in FIG. 4). In contrast, the ³¹P T₂ of the probe was not measurably affected by the same level of Mn²⁺ in the presence of the RNA (filled squares in FIG. 4). These results indicated that Mn²⁺ was effectively sequestered by the RNA and that, once sequestered, Mn²⁺ ions did not affect the relaxation properties of the probe ion.

Example 5 Determining the Affinity of the RNA for Mn²⁺

Example 4 demonstrated that the affinity of the 38 nt ARE construct for Mn²⁺ was sufficient to reduce the level of free Mn²⁺ from 5.3 to less than 1 μM. To estimate the binding affinity of the nucleic acid for Mn²⁺, samples containing the probe ion (EtOPH, 5 mM) and Mn²⁺ (5.3 μM) were treated with aliquots of the RNA construct (final concentrations of 0, 1.4, 2.9, 4, 6, 10, 14, 58, and 232 μM), and the values of the probe ion ³¹P T₂ were measured for each sample as in Example 3. A plot of reciprocal T₂ versus RNA concentration (FIG. 5) shows that metal ion sequestration was efficient for this sequence well below 10 μM. This figure also shows that more than one metal ion was bound per molecule of nucleic acid under these conditions.

Example 6 Determining the Affinity of a Drug Candidate for RNA

To determine the affinity of an RNA-binding drug candidate, MES10094, disclosed in U.S. application Ser. No. 10/117,955 filed on Apr. 8, 2002, for the 38 nt RNA, a sample containing Mn²⁺ (5.3 μM), probe (5 mM), and RNA (3.6 μM) was treated with a concentrated solution of MES 10094. The effect of increasing concentration of the drug lead on the ³¹P T₂, measured as in Example 3, is presented in FIG. 6. This figure clearly shows that addition of MES 10094 resulted in a pronounced increase in the rate of probe ion ³¹P T₂ relaxation. This result was consistent with the drug candidate displacing a fraction of the bound Mn²⁺ from the RNA. The data in FIG. 6 indicated that the K_(D) for metal displacement by MES 10094 under these conditions was on the order of 30 μM, which was consistent with values for inhibition of AUF1 binding to the RNA by MES 10094.

Example 7 Determining the Affinity of a Drug Candidate for a Species that Binds to RNA

To determine the affinity of a drug candidate for an RNA-binding species, e.g., a protein, a sample containing Mn²⁺ (5.3 μM), probe (5 mM), RNA-binding species (over a concentration range that spans an order of magnitude greater than and less than the expected K_(d)), and RNA (3.6 μM) is treated with a drug candidate. The effect of increasing concentration of the drug lead on the ³¹P T₂, measured as in Example 3, is then determined. The addition of a successful drug lead results in a pronounced decrease in the rate of probe ion ³¹P T₂ relaxation. This result is consistent with the drug candidate preventing the binding of the RNA-binding species and allowing a fraction of the free Mn²⁺ to bind to the RNA. The K_(D) for binding to the RNA-binding species under these conditions is determined from curve fitting the data.

Example 8 Screening a Molecular Library for Drug Candidates

Species in a molecular library are screened to determine drug candidates that bind to RNA or inhibit binding of other species to RNA. Screening for RNA-binding candidates proceeds as in Example 6, and screening for candidates that inhibit binding of other species to RNA proceeds as in Example 7. Several compounds may be screened at once. If a mixture contains a drug candidate, the individual species are then tested to determine the active species.

Example 9 Determining Non-Sequence Specific Association of Metals Ions with RNA

To establish the effects of non-specific interactions, metal ion association with a 31-nucleotide poly-U RNA (U₃₁) was compared to association with a 31 nucleotide ARE construct. The effects of these two 31-nucleotide RNA constructs on the availability of Mn²⁺ in low salt (˜12 mM Na⁺) solutions of 5 mM PIPES, pH 7.2, as measured in Example 3, are shown in FIG. 7. The effects of U₃₁ are represented by diamonds while those of the 31-nt ARE construct are represented by triangles. This figure clearly demonstrates the base specific nature of metal binding. Solid lines represent behavior predicted by a model wherein a single binding site existed with K_(d) values of 38 (upper line) and 2.7 μM (lower line). Dashed line (a) represents behavior predicted for a model where the ARE construct bound a single metal ion with high affinity.

This system was used to investigate the effects of added electrolytes on metal binding. While added sodium chloride had little effect on Mn²⁺ binding by the 31-nt ARE, addition of 100-mM Na⁺ resulted in negation of the effects of the U₃₁ construct. This result shows that Na⁺ competes effectively with Mn²⁺ for association with the U₃₁ construct but not with the ARE construct. The differences between the behaviors of U₃₁ and the ARE construct indicate that the ARE construct has specific binding sites for divalent cations, such as Mn²⁺. In the higher salt solution, 50 μM RNA had about half the effect on magnetic relaxation than it did in the lower salt solution (data not shown).

Example 10 Titration of Mn²⁺ with A-Site RNA Under Low Salt Conditions

In solutions containing 5 mM each of the sodium salts of MeOPH and PIPES buffer (pH 7.2), the concentration of sodium ion is calculated to be ˜12.5 mM. Addition of a 27-nt A-site construct to a solution of Mn²⁺ under these conditions caused the uptake of multiple Mn²⁺ ions per molecule of RNA, as measured as in Example 3. The data are presented in FIG. 8. The behavior predicted for tight binding in a 1:1 stoichiometry is presented as dashed line (a). The series of unbroken curves illustrates the behavior predicted by binding different numbers of metal ions at assumed values of K_(d). In this model, all sites were assumed to have the same K_(d) and behave independently of whether other sites were occupied. The lowest curve represents binding of four Mn²⁺ ions with a K_(d) of 4.6 μM. The highest curve represents binding of 8 Mn²⁺ ions with a K_(d) of 32 μM.

Example 11 Displacement of Metal Ions from the A-Site by Neomycin

FIG. 9 shows the effect of titration of a solution of a 27-nt A-site RNA construct (27 μM), complexed with Mn²⁺ (16 μM), with neomycin, measured as in Example 3. Data in this figure show that metal ions were displaced by addition of the aminoglycoside drug, neomycin, as was suggested by Mikkelsen et al (Mikkelsen, N. E. et al. Nature Struct. Biol. 2001, 8:510-514). The data shown in FIG. 9 were most consistent with a model where three neomycin molecules were bound to each RNA molecule with subsequent release of Mn²⁺. Release of Mn²⁺ resulted in an increase in the relaxation rate of the probe ion phosphorus nucleus.

Example 12 The Effects of Electrolytes on Magnetic Relaxation in Solutions of Mn²⁺ and RNA

The effect of K⁺ ion concentration on relaxation enhancement is shown in FIG. 10. While the addition of KCl solution resulted in an initial increase in relaxation enhancement, measured as in Example 3, after the concentration of monovalent ions exceeds about 40 mM, addition of more KCl had little effect. This apparent saturation effect could have one of two possible origins: the monovalent ions were only able to displace some percentage of the divalent ions from their binding sites, or at sufficiently high concentrations, monovalent ions associated with the RNA, neutralizing its negative charge. If the latter occurs, then relaxation of the phosphorous nucleus by the coordinated Mn²⁺ becomes possible.

Example 13 Determining the Effects of Potassium Ion on the Shapes of Titration Curves

The effects of 140 mM K⁺ on the curves obtained when solutions of Mn²⁺ are titrated with the 27-nt A-site construct are presented in FIG. 11. In contrast to the behavior observed in low salt, titrations in 140 mM K⁺ did not result in complete loss of relaxation enhancement, measured as in Example 3. A comparison of titrations run in 3 and 6 μM Mn²⁺ solutions shows that impurities introduced with the KCl or the buffer were not responsible for the residual relaxation enhancement. These results were most consistent with a model where association of monovalent ions with the A-site RNA resulted in a significant decrease in charge density, and as a result, the probe ion was able to contact the Mn²⁺ while bound to the nucleic acid.

Example 14 Determining the Number of High Affinity Metal Binding Positions on RNA

Under suitable conditions, it will be possible to determine the number of metal ions that are tightly bound by a given nucleic acid. Titration of a solution of the nucleic acid into a solution containing the paramagnetic metal ion and the probe ion will result in a decrease in the availability of the metal with the result that it will decrease the rate of T₂ relaxation of the probe nuclei, measured as in Example 3. The change in free metal concentration can be determined from the change in the relaxation rate. The following relationship applies: 1/T _(2,a)−1/T _(2,b) =k{[M] _(a) −[M] _(b)} where the subscripts a and b refer to solutions a and b, and k is a constant. For Mn²⁺ solutions k is equal to the second order rate constant for reaction with the probe ion, for MeOPH, this value is 5.8×10⁶ M⁻¹s⁻¹. Plotting the concentration of added nucleic acid versus the change in metal concentration will give a curve where the initial slope is equal to the stoichiometric ratio of metal ions bound per nucleic acid. To prevent interference from non-specific metal binding, these experiments may be performed at varying ionic strengths using an inert electrolyte such as ammonium acetate.

Example 15 Developing Structure Activity Relationships (SAR's) from Affinity Data

Using affinity data, structure activity relationships are developed to refine drug leads by established methods (Hajduik, P. J., et al. Quarterly Rev. Biophys. 1999, 32:211-240; Moore, J. M. Current Opin. Biotech., 1999, 10:54-58).

Example 16 Displacement of Mn²⁺ from RNA

NMR spectra were recorded on either a Varian Mercury 200 MHz, or a Bruker Avance DRX 500 MHz NMR spectrometer. Transverse relaxation rates (R₂=1/T₂) were measured indirectly by exploiting the strong scalar coupling between the phosphorus and the phosphorus bound hydrogen (J_(HP)=630 Hz). The one dimensional pulse sequence is described in FIG. 12.

RNA constructs were purchased from Dharmacon (Lafayette, Colo.) already gel purified and desalted. The samples were washed repeatedly, first with 1 M NaCl, and then with H₂O, using a centricon filtration device. Samples were subsequently lyophylized and reconstituted in D₂O prior to use. Neomycin b was purchased from Sigma (St. Louis, Mo.) and was used without further purification. The K+ salt of MeOPH was prepared by hydrolysis of (MeO)₂P(H)O (Aldrich, St. Louis, Mo.) with KOH solution. The reaction was monitored by pH, and was evaporated to dryness in vacuo. Similarly, K₂HPO₃ was prepared by neutralization of phosphorus acid (Aldrich) with KOH. Samples were pure by ¹H and ³¹P NMR and were used without further purification. The RSG1.2 peptide (Tan, R.; Frankel, A. D., Biochemistry 1994,33: 14579-14585) was prepared by Synpep, Inc (Dublin, Calif.), with a TAMRA label on the N-terminus. All NMR studies were performed in D₂O using PIPES as a non-complexing ionic buffer (Yu, Q.; Kandegedara, A.; Xu, Y.; Rorabacher, D. B., Ana.l Biochem. 1997, 253: 50-56). The buffer was prepared as the K⁺ salt by neutralization of the free acid with KOH.

Mn²⁺ binding by RNA constructs, and its displacement by either K⁺ or Mg²⁺. Samples containing MeOPH (5 mM) and PIPES buffer (5 mM, pH=7.2), and 3 μM Mn²⁺ were titrated with each RNA. The ³¹P transverse relaxation rates (R₂=1/T₂) of the probe in the resulting solutions were measured. Plots of R₂ versus [RNA] were prepared. The effects of [K⁺] and [Mg²⁺] on Mn²⁺ binding were determined by titrating similar solutions containing buffer, MeOPH, Mn²⁺, and one of the RNAs (10 to 30 μM) with solutions of either KCl or MgCl₂, and monitoring the relaxation rate of the probe as a function of cation concentration. The effects of [K⁺] were studied over the range of 12.5 to 150 mM (intercellular K⁺ is reportedly 140 mM). Mn²⁺ displacements from each of the hairpins by Mg²⁺, neomycin b, and RSG1.2 were studied in the absence of added KCl and with sufficient KCl added to bring the total [K⁺] to 100 mM. The compounds employed in this example are shown in FIG. 13.

Displacement of Mn²⁺ from RNA by RSG1.2, or neomycin b: Binding of RSG1.2 and neomycin b to each of the hairpins was studied at [RNA] between 20 and 30 μM, and again at [RNA] ˜3 μM. The higher concentration studies were performed in a manner identical to that described above for the Mg²⁺ exchange reactions. For the low concentration studies, HPO₃ ²⁻ (20 mM) was used as the probe ion. Reactions were run in 10 mM PIPES buffer, with 45 mM KCl and [Mn²⁺] between 50 and 150 nM. The pH of the samples was maintained at 7.8 in these experiments. Studies utilizing HPO₃ ²⁻ are impractical at lower pH where the probe undergoes dynamic proton exchange (pK_(A)=6.0) leading to significant shortening of the diamagnetic ³¹P T₂.

Fluorescence polarization studies of RSG1.2/RNA binding: Samples containing the N-terminally TAMRA labeled peptide, RSG1.2 (3 nM) and either RRE1 or RRE2 (concentrations ranging from 0.1 to 200 nM) were prepared in Reaction Buffer (10 mM Hepes-KOH pH 7.5; 150 mM KCl; 5 mM MgCl₂; 1 mM DTT; 1% glycerol; 50 μg/ml BSA; 100 μg/ml Hen-Egg Lysozyme). Each sample was irradiated at 530 nM and the polarization of the fluorescent emission at 580 nM was recorded using a LJL Analyst (Molecular Devices Corp. Sunnyvale, Calif.). Measurements repeated at 1, 15, and 30 min showed no evidence of change with time.

Measurable Mn²⁺ binding occurs under a useful range of [RNA]. The sensitivities of the ³¹P T₂ NMR relaxation rates of phospite (HPO₃ ²⁻) and methyl phosphite (MeOPH) to Mn²⁺ make it possible to measure [Mn²⁺] accurately at sub-micromolar levels (FIG. 14) (Summers et al. Inorg. Chem., 2001, 40: 6547-6554). Titration of each of the four RNAs into solutions containing Mn²⁺ (3 μM), MeOPH (5 mM), and PIPES buffer (5 mM, pH 7.2) caused a diminution of the MeOPH ³¹P transverse relaxation rate (R2), indicating that the RNAs sequestered the Mn²⁺. The effect of the A-site construct on free [Mn²⁺] (FIG. 15) is typical. In 12 mM K⁺, the three hairpins bound half the available Mn²⁺ at much lower concentrations (3 to 7 μM) than was required for U31 (˜50 μM). At 100 μM, the affinity of each hairpin RNA was sufficient that relaxation enhancement of the probe by 3 μM Mn²⁺ was undetectable. Since efficient relaxation enhancement requires inner sphere contact between MeOPH and the Mn²⁺ ion (Summers et al. Inorg. Chem., 2001, 40: 6547-6554), this result indicates that the anionic probe does not contact the RNA complexed metal ion. Thus, the ³¹P T₂ relaxation enhancement of MeOPH can be used to measure the concentration of free Mn²⁺ ion without interference by RNA complexed Mn²⁺.

While these experiments provide an accurate measure of the concentration of free Mn²⁺, the certainty of Mn²⁺ dissociation constants (K_(d,Mn)) derived from such data is limited by the uncertainty in the number of discreet binding sites. The line in FIG. 15 was produced assuming that the RNA has 7 non-interacting binding sites, each with K_(d,Mn)=25 μM. We note, however, that the data fit just as well to a model with 8 or more binding sites having higher K_(d,Mn) values. A Scatchard analysis of binding data would require knowledge of RNA saturation which is not available from this technique. Additional uncertainty is introduced by the potential presence of trace impurities (diamagnetic metal ions, and/or high affinity chelating agents such as EDTA) in the RNA samples. We feel that our K⁺, Mg²⁺, neomcyin b, and RSG1.2 samples are not nearly as prone to contamination as the RNA samples and have greater confidence in values derived from experiments wherein the concentration of the cation is varied. The 25 μM value is well within the range of dissociation constants published for Mn²⁺/RNA interactions: in 0.1 M NaCl, the hammerhead ribozyme reportedly binds four Mn²⁺ ions with K_(d,Mn) ˜4 μM and another five with K_(d,Mn) ˜460 μM (Hoogstraten et al. J. Am. Chem. Soc., 2002, 124: 834-842).

As observed in earlier studies, Mn²⁺/RNA binding was strongly influenced by the concentration of monovalent ions. At [K⁺] <20 mM, addition of KCl solution results in increased relaxation enhancement, above 40 mM, however, the K⁺ association becomes saturated and further addition of KCl had little effect. The effect of [K⁺] on Mn²⁺ binding by the A-site construct is presented in FIG. 16. The effects of K⁺ on Mn²⁺ binding by the RNAs were sequence dependent. While 30 mM K⁺ displaced all the Mn²⁺ from U₃₁, 150 mM K⁺ did not displace all the Mn²⁺ from any of the three hairpins. This result indicates that the hairpins contain discrete binding sites that are selective for divalent metals and that U₃₁ does not. We considered the possibility that high [K⁺] might allow contact between the probe ion and the RNA bound Mn²⁺. This hypothesis was inconsistent with the results of experiments comparing the relaxation enhancements of the two probes; MeOPH and HPO₃ ²⁻. The two probes (which have different electronic charges) should differ in sensitivity to the electronic environment of the Mn²⁺. This reasoning was borne out by experiments comparing the relative sensitivities of MeOPH and HPO₃ ²⁻ toward relaxation by Mn²⁺ in the presence and absence of EDTA. Relaxation of the di-anionic probe HPO₃ ²⁻ by the anionic metal complex (MnEDTA²⁻) was found to be significantly slower than that of the mono-anionic probe (MeOPH) (Results not shown). While addition of K⁺ to Mn²⁺ containing solutions of RRE1, caused an increase in the relaxation rates of both probes, the ratio of the two remained equal to that observed in the absence of the RNA. Since the electronic charge environment surrounding the complexed Mn²⁺ should be significantly different than that of the free ion, this result indicates that addition of K⁺ causes an increase in the concentration of free Mn²⁺, which is the sole species responsible for probe nucleus relaxation in these experiments. The decrease in Mn²⁺ affinity is likely to stem from a combination of two effects: First, K⁺ is able to compete with Mn²⁺ for non-specific electrostatic interactions, and second, neutralization of the anionic charge causes a decrease in the affinity of specific divalent metal sites.

Mn²⁺ is displaced from RNA by Mg²⁺ in competition experiments. To determine whether Mn²⁺ was bound at sites on the RNA molecules that bind Mg²⁺ in vivo, we titrated solutions containing Mn²⁺ and the RNAs with MgCl₂ solution and monitored the effect using the PhoRE technique. The effect of Mg²⁺ on Mn²⁺ binding by U₃₁ was that expected for competition between two identical cations for association with an indiscriminate poly-anion; the probe R₂ increased with [Mg²⁺] until the concentrations of the two ions were similar. After the [Mg²⁺] had exceeded about twice the [Mn²⁺], addition of more Mg²⁺ had no measurable effect.

Mn²⁺ bound by the hairpins was displaced by Mg²⁺ in a manner more consistent with the metals being bound in a well defined complex. The effects of [Mg²⁺] on Mn²⁺ binding by RRE1 at two different [K⁺] are presented in FIG. 17. Titration curves were interpreted in terms of a model that assumes that [Mn²⁺]<<K_(d,Mn) and that the Mg²⁺ binding equilibrium is governed by the Hill equation. Under these conditions the effect of [Mg²⁺] on the observed relaxation rate (R_(2,obs)) is governed by Eq (1): (Q−Q ₀)/Q ₀=(1/K_(d,Mg))[Mg]^(n)   (1)

where Q=(R_(2,obs)−R_(2,dia))/(R_(2,max)−R_(2,obs)), R_(2,dia) and R_(2,max) represent the values of R₂ in diamagnetic solutions and the maximum value observed, respectively. The term Q₀ (defined as Q₀=K_(d,Mn)/RNA) arises from the competitive nature of the experiment, and represents the value of Q observed in the absence of added Mg²⁺. The presence of Q₀ in Eq (1) introduces a minor complication in the interpretation of the data which can be illustrated by considering the data presented in FIG. 17. While the concentrations of Mg²⁺ required to release half the bound Mn²⁺ were similar for the two experiments (300 and 600 μM), Q₀ values were significantly different. As a result K_(d,Mg) determined in 25 mM K⁺ was considerably lower than in 100 mM K⁺ (64 versus 360 μM, Table 1). TABLE 1 Equilibrium coefficients for Mg²⁺ binding by RNA constructs. K_(d, Mg) (μM) (Hill Coefficient) RNA 25 mM K⁺ 100 mM K⁺ U₃₁ none A-site 55 (0.8) 154 (1.0) RRE1 64 (2.8) 360 (1.5) RRE2 344 (1.0)

Using the analysis described above, values of K_(d,Mg) and n were determined for A-site and RRE1 at low [K⁺] and at saturating [K⁺] (Table 1). Like RRE1, the A-site also showed a marked decrease in Mg²⁺ affinity at the higher [K⁺]. The decrease in Mg²⁺ affinity at the higher [K⁺] mirrors the decrease in Mn²⁺ affinity noted above. All the values in Table 1 are well within the range of those found in the literature; values of K_(d,Mg) ranging from 1 μM to 2 mM have been reported for transfer RNAs alone (Schimmel et al. Ann Rev. Biophys. Bioeng., 1980, 9: 181-221).

Neomycin b reacted with each of the hairpins, causing a release of Mn²⁺. The Mn²⁺ release was proportional to the added neomycin until the RNA was saturated. After saturation, continued addition of neomycin had no effect on MeOPH relaxation (FIG. 18). The ratio of neomycin to RNA at the saturation point was dependant on the RNA sequence, [K⁺], and [RNA]. At [RNA]=2.7 μM (100 mM K⁺), the A-site construct bound a single equivalent of neomycin (FIG. 18). At [RNA]=27 μM, however, the same construct bound 3 equivalents (data not shown). Both RRE1 and RRE2 constructs bound multiple equivalents of neomycin under each condition studied. Thus, of the three hairpins, only the A-site construct bound neomycin in a 1:1 complex, and only at RNA<3 μM. The low selectivity for neomycin binding should not be surprising since the antibiotic is known to bind a wide variety of RNAs with varying affinities (Hendrix et al. J Am. Chem. Soc., 1997, 119: 3641-3648; Sannes-Lowery et al. Anal. Biochem., 2000, 280: 264-271.). We note that another RRE1 model bound three equivalents of neomycin b (Harada et al. Nature, 1996, 380: 175-179).

Binding RSG1.2 peptide to RNA constructs was also strongly dependent on RNA sequence, [RNA] and [K⁺]. At <3 μM RNA, 100 mM K⁺, the RRE1 construct bound a single equivalent of RSG1.2 (FIG. 19). Under these conditions neither the RRE2 construct, nor the A-site bound the peptide. At higher RNA (>20 μM), each RRE construct bound multiple equivalents of RSG1.2, releasing Mn²⁺, resulting in precipitation of the RNA/peptide complex. The results of our PhoRE studies of RSG1.2/RNA binding are consistent with those of our fluorescence polarization studies of this system. The effects of RRE1 and RRE2 on fluorescence polarization of TAMRA labeled RSG1.2 are presented in FIG. 20. Low levels of RRE1 cause an increase in polarization consistent with complexation of the peptide and an increase in effective mass. A similar level of polarization requires a fifty fold greater concentration of RRE2, indicating a weaker interaction between the peptide and this RNA.

Our results demonstrate that PhoRE represents a viable method for studying the interactions of metal ions, small molecules, and peptides with nucleic acids. We describe evidence for discreet divalent metal binding sites on three hairpin RNAs. We found that Mg²⁺ is able to compete with Mn²⁺ at physiological concentrations, indicating that small molecules, peptides, or proteins that displaces Mn²⁺ from an RNA should bind in vivo by displacing Mg²⁺.

Other Embodiments

Modifications and variations of the described methods of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific desirable embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention, which are obvious to those skilled in the field of chemistry or related fields, are intended to be within the scope of the invention.

All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually to be incorporated by reference.

Other embodiments are in the claims. 

1. A method of detecting the binding of a species to a biopolymer other than a protein, said method comprising the steps of: (a) measuring a magnetic relaxation property of a probe in a first solution using nuclear magnetic resonance spectroscopy, wherein said first solution comprises said biopolymer, a first concentration of said species, a paramagnetic metal ion, and said probe; (b) measuring the magnetic relaxation property of said probe in a second solution using nuclear magnetic resonance spectroscopy, wherein said second solution comprises said biopolymer, a second concentration of said species, a paramagnetic metal ion, and said probe; and (c) comparing the relaxation property measured in step (a) with the relaxation property measured in step (b), wherein a difference in said relaxation properties indicates the binding of said species to said biopolymer.
 2. The method of claim 1, wherein, in step (c), said magnetic relaxation properties of said probe are correlated with said first and second concentrations of said species, thereby quantifying the binding of said species to said biopolymer.
 3. The method of claim 1, wherein said first concentration is 0.0 μM. 4.-5. (canceled)
 6. The method of claim 1, wherein said species is a candidate therapeutic agent. 7.-9. (canceled)
 10. The method of claim 1, wherein said paramagnetic metal ion is bound to said biopolymer.
 11. The method of claim 1, wherein said probe comprises an X—H bond, wherein X is an NMR-active nucleus.
 12. The method of claim 11, wherein X is ³¹P.
 13. The method of claim 12, wherein said probe is methylphosphite, ethylphosphite, or ethylphosphonite.
 14. The method of claim 11, wherein said magnetic relaxation property of X is indirectly detected using X edited, ¹H detected NMR spectroscopy.
 15. (canceled)
 16. The method of claim 1, wherein said magnetic relaxation property is the T₂ relaxation of a nucleus of said probe.
 17. The method of claim 1, wherein said biopolymer comprises a nucleic acid.
 18. The method of claim 1, wherein said biopolymer comprises a polypeptide.
 19. The method of claim 1, wherein said biopolymer comprises a polysaccharide.
 20. A method of detecting the binding of a paramagnetic metal ion to a biopolymer other than a protein, said method comprising the steps of: (a) measuring a magnetic relaxation property of a probe in a first solution using nuclear magnetic resonance spectroscopy, wherein said first solution comprises a first concentration of said paramagnetic metal ion, said biopolymer, and said probe; (b) measuring the magnetic relaxation property of said probe in a second solution using nuclear magnetic resonance spectroscopy, wherein said second solution comprises a second concentration of said paramagnetic metal ion, said biopolymer, and said probe; and (c) comparing the relaxation property measured in step (a) with the relaxation property measured in step (b), wherein a difference in said relaxation properties indicates the binding of said paramagnetic metal ion to said biopolymer.
 21. The method of claim 20, wherein, in step (c), said magnetic relaxation properties of said probe are correlated with said first and second concentrations of said nucleic acid, thereby quantifying the binding of said paramagnetic metal ion to said nucleic acid.
 22. The method of claim 20, wherein said first concentration is 0.0 μM.
 23. (canceled)
 24. The method of claim 1, wherein said probe comprises an X—H bond, wherein X is an NMR-active nucleus.
 25. The method of claim 18, wherein X is ³¹P.
 26. The method of claim 25, wherein said probe is methylphosphite, ethylphosphite, or ethylphosphonite.
 27. A method of determining the effect of a first species on the binding of a second species to a biopolymer other than a protein, said method comprising the steps of: (a) measuring a magnetic relaxation property of a probe in a first solution using nuclear magnetic resonance spectroscopy, wherein said first solution comprises a first concentration of said first species, said biopolymer, said second species that binds to said biopolymer, a paramagnetic metal ion, and a probe; (b) measuring the magnetic relaxation property of said probe in a second solution using nuclear magnetic resonance spectroscopy, wherein said second solution comprises a second concentration of said first species, said biopolymer, said second species, said paramagnetic metal ion, and said probe; and (c) comparing the relaxation property measured in step (a) with the relaxation property measured in step (b), wherein a difference in said relaxation properties indicates the inhibition of the binding of said second species to said biopolymer.
 28. The method of claim 27, wherein, in step (c), said magnetic relaxation properties of said probe are correlated with said first and second concentrations of said first species, thereby quantifying the effect of said first species on the binding of said second species to said biopolymer.
 29. The method of claim 27, wherein said first concentration is 0.0 μM. 30.-31. (canceled)
 32. The method of claim 27, wherein said first species or said second species is a candidate therapeutic agent. 33.-35. (canceled)
 36. The method of claim 27, wherein said paramagnetic metal ion is bound to said biopolymer.
 37. The method of claim 27, wherein said probe comprises an X—H bond, wherein X is an NMR-active nucleus.
 38. The method of claim 27, wherein X is ³¹P.
 39. The method of claim 38, wherein said probe is methylphosphite, ethylphosphite, or ethylphosphonite.
 40. A method of detecting the availability of a paramagnetic metal ion in a solution comprising a biopolymer other than a protein, said method comprising the steps of: (a) providing a solution comprising said biopolymer, a probe, and said paramagnetic metal ion and (b) measuring a magnetic relaxation property of said probe in said solution using nuclear magnetic resonance spectroscopy, wherein the magnitude of said magnetic property is indicative of the availability of said paramagnetic ion in said solution.
 41. The method of claim 40, wherein said paramagnetic metal ion is bound to said biopolymer. 